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| Additional findings_Paediatric v1.0 | BCL9 | Gene migrated from ENSG00000116128 to ENSG00000116128 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | BCL9 |
Zornitza Stark gene: BCL9 was added gene: BCL9 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: BCL9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: BCL9 were set to Congenital heart disease |
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